Product Details

SNP ID

rs200117955

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:35253755 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAATAAGGGCTGAGCTCCGGCTGA[A/C]GGCCTTCCCACATTCTCCACATTCA

Phenotype

MIM: 609601

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

ZNF397 PubMed Links

Gene Details

Gene

ZNF397

Gene Name

zinc finger protein 397

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135178.2	1597	Intron			NP_001128650.1
NM_032347.2	1597	Intron			NP_115723.1
XM_006722558.2	1597	UTR 3			XP_006722621.1
XM_011526229.2	1597	UTR 3			XP_011524531.1
XM_011526230.2	1597	UTR 3			XP_011524532.1
XM_011526231.2	1597	UTR 3			XP_011524533.1
XM_017026042.1	1597	UTR 3			XP_016881531.1

Gene

ZSCAN30

Gene Name

zinc finger and SCAN domain containing 30

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001112734.3	1597	Missense Mutation	GTC,TTC	V394F	NP_001106205.1
NM_001166012.2	1597	Missense Mutation	GTC,TTC	V394F	NP_001159484.1
NM_001288711.1	1597	Missense Mutation	GTC,TTC	V207F	NP_001275640.1
XM_005258183.4	1597	Missense Mutation	GTC,TTC	V394F	XP_005258240.1
XM_006722371.3	1597	Missense Mutation	GTC,TTC	V394F	XP_006722434.1
XM_011525789.2	1597	Missense Mutation	GTC,TTC	V207F	XP_011524091.1
XM_017025515.1	1597	Missense Mutation	GTC,TTC	V394F	XP_016881004.1
XM_017025516.1	1597	Missense Mutation	GTC,TTC	V251F	XP_016881005.1
XM_017025517.1	1597	Missense Mutation	GTC,TTC	V251F	XP_016881006.1
XM_017025518.1	1597	Missense Mutation	GTC,TTC	V251F	XP_016881007.1
XM_017025519.1	1597	Missense Mutation	GTC,TTC	V207F	XP_016881008.1
XM_017025520.1	1597	Missense Mutation	GTC,TTC	V207F	XP_016881009.1
XM_017025521.1	1597	Missense Mutation	GTC,TTC	V207F	XP_016881010.1
XM_017025522.1	1597	Missense Mutation	GTC,TTC	V207F	XP_016881011.1

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